A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522826



Internal ID21847185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65750960..65873041hg38UCSC Ensembl
chr2:65978094..66100175hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38122082
hg19122082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5989793
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522826
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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